2,5,9-Trimethyldecane

Details

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Internal ID bc38049b-284c-458f-bf48-e11ef9e94821
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2,5,9-trimethyldecane
SMILES (Canonical) CC(C)CCCC(C)CCC(C)C
SMILES (Isomeric) CC(C)CCCC(C)CCC(C)C
InChI InChI=1S/C13H28/c1-11(2)7-6-8-13(5)10-9-12(3)4/h11-13H,6-10H2,1-5H3
InChI Key YKAQOUURBLPHIN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H28
Molecular Weight 184.36 g/mol
Exact Mass 184.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.40
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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Decane, 2,5,9-trimethyl-
62108-22-9
2,5,9-trimethyl-decane
2,5,9-Trimethyldecane #
DTXSID30334825
YKAQOUURBLPHIN-UHFFFAOYSA-N

2D Structure

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2D Structure of 2,5,9-Trimethyldecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.8635 86.35%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4160 41.60%
OATP2B1 inhibitior - 0.8478 84.78%
OATP1B1 inhibitior + 0.9762 97.62%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9569 95.69%
P-glycoprotein inhibitior - 0.9488 94.88%
P-glycoprotein substrate - 0.8667 86.67%
CYP3A4 substrate - 0.6896 68.96%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9879 98.79%
CYP2C9 inhibition - 0.9393 93.93%
CYP2C19 inhibition - 0.9537 95.37%
CYP2D6 inhibition - 0.9595 95.95%
CYP1A2 inhibition - 0.7915 79.15%
CYP2C8 inhibition - 0.9932 99.32%
CYP inhibitory promiscuity - 0.8953 89.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6061 60.61%
Eye corrosion + 0.9879 98.79%
Eye irritation + 0.9842 98.42%
Skin irritation + 0.8683 86.83%
Skin corrosion - 0.9821 98.21%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5753 57.53%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5802 58.02%
skin sensitisation + 0.9397 93.97%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity - 0.9689 96.89%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.5822 58.22%
Acute Oral Toxicity (c) III 0.6311 63.11%
Estrogen receptor binding - 0.8820 88.20%
Androgen receptor binding - 0.9288 92.88%
Thyroid receptor binding - 0.6429 64.29%
Glucocorticoid receptor binding - 0.8793 87.93%
Aromatase binding - 0.7903 79.03%
PPAR gamma - 0.9004 90.04%
Honey bee toxicity - 0.9668 96.68%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9700 97.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 87.54% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 87.06% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.32% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 84.49% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.26% 97.29%
CHEMBL260 Q16539 MAP kinase p38 alpha 81.20% 97.78%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.03% 90.71%
CHEMBL333 P08253 Matrix metalloproteinase-2 81.01% 96.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.18% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 522020
NPASS NPC227514